Canonical Allele Identifier: CA508089375
Gene: NTF4 HGNC NCBI

Linked Data

gnomAD v4: 19-49060810-C-A
MyVariant Identifiers: chr19:g.49564067C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060810C>A , CM000681.2:g.49060810C>A GRCh38
NC_000019.9:g.49564067C>A , CM000681.1:g.49564067C>A GRCh37
NC_000019.8:g.54255879C>A NCBI36
NG_016289.1:g.8058G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+945G>T ENSP00000470689.1:n.243+945G>T
XM_011527575.1:c.-58G>T XP_011525877.1:n.-58G>T
XR_001753693.1:n.879+354G>T
XR_001753694.1:n.880-1G>T
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